CD14, CD14 molecule, 929

N. diseases: 551; N. variants: 8
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0031099
Disease: Periodontitis
Periodontitis 		Stomatognathic Diseases 0.030 0.667 3 2016 2019
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.020 1.000 2 2014 2015
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.020 1.000 2 2014 2015
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.020 1.000 2 2011 2012
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.020 1.000 2 2009 2019
dbSNP: rs2563298
rs2563298 		0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26
CUI: C0036690
Disease: Septicemia
Septicemia 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2014 2014
dbSNP: rs2563298
rs2563298 		0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26
CUI: C0243026
Disease: Sepsis
Sepsis 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2014 2014
dbSNP: rs2563298
rs2563298 		0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease 		Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2563298
rs2563298 		0.851 0.200 5 140631730 3 prime UTR variant C/A snv 0.26
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma 		Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C1719498
Disease: Generalized chronic periodontitis
Generalized chronic periodontitis 		Stomatognathic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0858617
Disease: Posterior subcapsular cataract
Posterior subcapsular cataract 		Eye Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0566602
Disease: Primary sclerosing cholangitis
Primary sclerosing cholangitis 		Digestive System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0947961
Disease: Atopic disorders
Atopic disorders 		0.010 1.000 1 2005 2005
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0005411
Disease: Biliary Atresia
Biliary Atresia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0155877
Disease: Allergic asthma
Allergic asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2569190
rs2569190 		0.620 0.560 5 140633331 intron variant A/G snv 0.57
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic 		Digestive System Diseases; Infections 0.010 1.000 1 2009 2009